A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109698



Internal ID21449613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165482057..165482057hg38UCSC Ensembl
chr2:166338567..166338567hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610706
Supporting Variants
SamplesHG01114
Known GenesCSRNP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109698
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer